US4408003A - Varnishes for glasscloth laminates, methods of their production and laminates made therefrom - Google Patents

Varnishes for glasscloth laminates, methods of their production and laminates made therefrom Download PDF

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US4408003A
US4408003A US06/311,647 US31164781A US4408003A US 4408003 A US4408003 A US 4408003A US 31164781 A US31164781 A US 31164781A US 4408003 A US4408003 A US 4408003A
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laminates
resin
varnish
parts
solvent
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US06/311,647
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Joseph G. Robinson
Sally A. Brain
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Coal Industry Patents Ltd
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Coal Industry Patents Ltd
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Assigned to COAL INDUSTRY (PATENTS) LIMITED reassignment COAL INDUSTRY (PATENTS) LIMITED ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: BRAIN, SALLY A., ROBINSON, JOSEPH G.
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09D161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/04Layered products comprising a layer of synthetic resin as impregnant, bonding, or embedding substance
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/24Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
    • C08J5/241Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres
    • C08J5/244Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using glass fibres
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/34Condensation polymers of aldehydes or ketones with monomers covered by at least two of the groups C08L61/04, C08L61/18 and C08L61/20
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00Printed circuits
    • H05K1/02Details
    • H05K1/03Use of materials for the substrate
    • H05K1/0313Organic insulating material
    • H05K1/032Organic insulating material consisting of one material
    • H05K1/0326Organic insulating material consisting of one material containing O
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2361/00Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
    • C08J2361/34Condensation polymers of aldehydes or ketones with monomers covered by at least two of the groups C08J2361/04, C08J2361/18, and C08J2361/20
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2926Coated or impregnated inorganic fiber fabric
    • Y10T442/2992Coated or impregnated glass fiber fabric

Definitions

  • the present invention relates to varnishes for use in the preparation of glass cloth laminates, and also to methods of preparing the varnishes and to laminates made from the varnishes.
  • the varnishes are prepared using toluene phenol formaldehyde (TFP) resins.
  • thermosetting resins which are stable at high temperatures (in the region from 200° to 250° C.) and which retain their mechanical properties at these temperatures.
  • These resins include polymides, poly (amide-imides), polybenzimidazoles and polyphenylenes. These resins are derived from expensive materials and are difficult to make. They have limited commercial acceptability either because of their high cost or because their chemical or physical properties are not adequate for their intended use.
  • a varnish for the preparation of glass cloth laminates comprising a mixture of a solution of 100 parts of a TFP resin having a number average molecular weight of about 1000 and an oxygen content of about 8% in from 60 to 65 parts of a C 4 to C 6 alkanone or a C 3 or C 4 alkanol, and a solution of from 8 to 12 parts of hexamethylene tetramine (hexamine) dissolved in a minimum amount of a solvent comprising water and a lower alkanol in a ratio of about 3:5.
  • a method of preparing the varnish comprising dissolving 100 parts of the TFP resin defined above in from 60 to 65 parts of a C 4 to C 6 alkanone or a C 3 or C 4 alkanol, dissolving from 8 to 12 parts of hexamine in a minimum amount of a solvent comprising water and a lower alkanol in a ratio of about 3:5, and mixing the two solutions.
  • the mixture of the two solutions is filtered before it is used as a varnish.
  • a glass cloth laminate made using the varnish according to the first aspect of the invention or made according to the second aspect of the invention.
  • the TFP resin is made according to the method described in our previously mentioned European application, and therefore contains a small proportion of low molecular weight material.
  • This component is able to wet the glasscloth substrate efficiently, enabling the laminate to be easily consolidated before it is cured. This results in a cured laminate of good thermal stability.
  • the alkanone may be 1,1-dimethylbutan-2-one or one of the pentanones, but is preferably butan-2-one.
  • the C 3 or C 4 alkanol may be a propanol, and is preferably iso-propanol.
  • the lower alkanol may be methanol, ethanol or a propanol, or mixtures of them, and is preferably industrial methylated spirit (IMS), which contains approximately 95% ethanol, 5% methanol and contaminant amounts of higher alcohols.
  • IMS industrial methylated spirit
  • the critical factors in the varnish and its preparation are the choice of solvent for the resin, the concentration of resin in its solvent and the hexamine solution. It has been found that solvents usually used in resin varnishes such as ethanol or acetone cannot be used to form satisfactory laminates with the particular resin used in the present invention. If the concentration of resin in the solution is not within the given range either a weak laminate which tends to delaminate will be formed, or the glass cloth will not be fully impregnated by the varnish and the resin will not cure properly. It must be ensured that the hexamine is fully dissolved in the water-lower alkanol solvent and that as little of the solvent as possible is used. The hexamine must also be evenly distributed throughout the final varnish.
  • the final laminates are envisaged as being useful as printed circuit boards and compressor blades for gas turbines.
  • the condensation resin was then subjected to distillation for 8 hours at a pot temperature of 200° C. under a pressure of 20 mm Hg. to produce an intermediate resin as the residue.
  • the intermediate resin was phenolated with phenol itself as follows. Phenol (22.5 kg) and 100% para-toluene sulphonic acid (165 g) were charged to a heated reactor fitted with a reflux condenser. When the reactor temperature reached 85° C., the intermediate resin (27.5 kg), maintained at about 50° C. to keep the resin mobile, was slowly dripped into the reactor. The resin addition took approximately 1 hour. The temperature of the mixture rose to about 118° C. during the addition. After all the resin had been added, the mixture was heated to about 140° C. and superheated steam at about 150° C. was passed through it to raise the softening point of the phenolated resin. When the softening point of the resin was 105° C. (determined by the Ring and Ball method) the phenolated resin was allowed to cool and was dried.
  • the phenolated resin had the properties given below:
  • the phenolated resin (100 parts) was then dissolved in sufficient IMS to give a 50% solution and hexamine (10 parts) (based on the weight of the phenolated resin) was added thereto. This provided a varnish which was used to make glasscloth laminates.
  • the impregnated sheets were freely suspended and air dried for about 1 hour after which they were pre-cured for a fixed time in an air circulating oven at 135° C. Each sheet was cut into 4 equal squares and the 20 sheets thus obtained were stacked one of top of each other between plates lined with aluminum foil. The stack of sheets was pressed at 150° C. in a hydraulic press. The initial pressure was 3.4 MN/mm 2 which was allowed to fall progressively to 1.13 MN/mm 2 over the 1 hour dwell period. At the end of this time the laminate was cooled to room temperature while still under pressure (1.13 MN/mm 2 ) and thereafter removed for post-curing.
  • Rectangular test pieces 12.5 mm wide and of length approximately 27 times their thickness milled from the cured laminates were supported at one end and freely suspended in an air oven at 175° C. and post-cured as follows.
  • TFP phenolated toluene formaldehyde
  • the TFP resin 100 parts was then dissolved in butane-2-one (63 parts).
  • Hexamine (10 parts) was dissolved in a minimum amount of water, in this case 14 parts of water, and IMS (23 parts) was added.
  • the hexamine solution was mixed thoroughly to ensure that all the hexamine was dissolved.
  • the TFP resin solution and the hexamine solution were then mixed intimately and filtered through muslin to produce a first varnish according to the invention.
  • the varnish was used to make glass cloth laminates.
  • the method of producing the laminates from the two varnishes according to the invention was the same as that described in Preparation 1, and included the same curing and post-curing schedule. At no time was there any evidence of cracking or blistering whichever varnish according to the invention was used and the laminates maintained their strength throughout the treatment period. Moreover, the cross-breaking strength of the laminates measured at 250° C. was relatively unchanged after ageing for up to 1000 h at 250° C.
  • glass cloth laminates made with varnishes according to the invention have equivalent properties to similar laminates made with a commercial resin, such as Xylok-210.

Abstract

The present invention relates to varnishes for use in the preparation of glasscloth laminates, methods of their production and laminates made therefrom.
The varnish is made by dissolving 100 parts of a TFP resin having a number average molecular weight of about 1000 and an oxygen content of about 8% in 60 to 65 parts of butan-2-one or isopropanol. 8 to 12 parts of hexamine are dissolved in a minimum quantity of a solvent comprising water and IMS in a ratio of about 3:5. The two solutions are thoroughly mixed and filtered to produce the varnish.
The varnish is used to prepare glasscloth laminates for use as printed circuit boards.

Description

The present invention relates to varnishes for use in the preparation of glass cloth laminates, and also to methods of preparing the varnishes and to laminates made from the varnishes. In particular, the varnishes are prepared using toluene phenol formaldehyde (TFP) resins.
Several thermosetting resins have been developed which are stable at high temperatures (in the region from 200° to 250° C.) and which retain their mechanical properties at these temperatures. These resins include polymides, poly (amide-imides), polybenzimidazoles and polyphenylenes. These resins are derived from expensive materials and are difficult to make. They have limited commercial acceptability either because of their high cost or because their chemical or physical properties are not adequate for their intended use.
These resins are required in various industries to form relatively strong laminated materials which will withstand temperatures up to about 250° C. without significant loss of their physical properties.
In view of their commercial unacceptability, other resins have been proposed to replace them in the manufacture of laminates. For instance Friedel Crafts resins, such as Xylok 210 made by Albright and Wilson, have been used to form laminates. This resin is expensive, and it has been an object of our research to find a cheaper alternative. It was discovered that TFP resins appeared to have the requisite properties, as disclosed in our published European Patent application No. 0017312. This described a method of preparing a TFP resin suitable for various laminating and other uses.
However when this resin was used to prepare glass cloth laminates, it was found that the laminates cracked and blistered during either curing or post-curing of the laminates, thus rendering them technically unacceptable. Therefore, research work was undertaken with a view to producing acceptable glass cloth laminates using TFP resins as the bonding agents. It was discovered that this could be achieved only by use of carefully selected varnishes which had compositions falling within narrow limits. If the varnish's composition fell outside these limits, the laminates cracked and blistered or did not have adequate physical properties.
According to a first aspect of the invention, there is provided a varnish for the preparation of glass cloth laminates, comprising a mixture of a solution of 100 parts of a TFP resin having a number average molecular weight of about 1000 and an oxygen content of about 8% in from 60 to 65 parts of a C4 to C6 alkanone or a C3 or C4 alkanol, and a solution of from 8 to 12 parts of hexamethylene tetramine (hexamine) dissolved in a minimum amount of a solvent comprising water and a lower alkanol in a ratio of about 3:5.
According to a second aspect of the invention there is provided a method of preparing the varnish comprising dissolving 100 parts of the TFP resin defined above in from 60 to 65 parts of a C4 to C6 alkanone or a C3 or C4 alkanol, dissolving from 8 to 12 parts of hexamine in a minimum amount of a solvent comprising water and a lower alkanol in a ratio of about 3:5, and mixing the two solutions. Preferably, the mixture of the two solutions is filtered before it is used as a varnish.
According to a third aspect of the invention there is provided a glass cloth laminate made using the varnish according to the first aspect of the invention or made according to the second aspect of the invention.
Preferably, the TFP resin is made according to the method described in our previously mentioned European application, and therefore contains a small proportion of low molecular weight material. This component is able to wet the glasscloth substrate efficiently, enabling the laminate to be easily consolidated before it is cured. This results in a cured laminate of good thermal stability.
The alkanone may be 1,1-dimethylbutan-2-one or one of the pentanones, but is preferably butan-2-one. The C3 or C4 alkanol may be a propanol, and is preferably iso-propanol. The lower alkanol may be methanol, ethanol or a propanol, or mixtures of them, and is preferably industrial methylated spirit (IMS), which contains approximately 95% ethanol, 5% methanol and contaminant amounts of higher alcohols.
The critical factors in the varnish and its preparation are the choice of solvent for the resin, the concentration of resin in its solvent and the hexamine solution. It has been found that solvents usually used in resin varnishes such as ethanol or acetone cannot be used to form satisfactory laminates with the particular resin used in the present invention. If the concentration of resin in the solution is not within the given range either a weak laminate which tends to delaminate will be formed, or the glass cloth will not be fully impregnated by the varnish and the resin will not cure properly. It must be ensured that the hexamine is fully dissolved in the water-lower alkanol solvent and that as little of the solvent as possible is used. The hexamine must also be evenly distributed throughout the final varnish. If these points are not observed laminates formed using the varnish will crack or blister. This is thought to be due to the fact that only using the parameters specified in the present invention is it possible to ensure that volatiles formed during the curing are able to escape from the laminate and that the resin is properly cured. However we do not wish to be limited to this explanation which of itself forms no part of the invention.
The final laminates are envisaged as being useful as printed circuit boards and compressor blades for gas turbines.
In this specification and the claims all parts, percentages and ratios are by weight unless otherwise indicated.
The present invention will now be illustrated, by way of example only, with reference to three preparations.
Preparation 1--Varnish made According to the Prior Art
A toluene-formaldehyde condensation resin was made by charging water (3.4 kg) and 77% sulphuric acid (18.7 kg) to a stirred reactor. The temperature of the acid was raised to about 35° C. and paraform `87` (28.2 kg) was added. The reactor was heated to about 60° C. and toluene (25 kg) was added (Molar ratios: formaldehyde to toluene=3:1; sulphuric acid to toluene=0.54:1). The reactor was heated to 90° C. and the toluene/water azeotrope allowed to reflux in a vertical condenser. The temperature of the reaction mixture rose during the reaction to about 102° C. and was held at this temperature for 3 hours. The reactor was then cooled, the aqueous layer separated off and the condensation resin water-washed until neutral. The condensation resin has an oxygen content of 11% and a number average molecular weight of 440.
The condensation resin was then subjected to distillation for 8 hours at a pot temperature of 200° C. under a pressure of 20 mm Hg. to produce an intermediate resin as the residue.
The intermediate resin was phenolated with phenol itself as follows. Phenol (22.5 kg) and 100% para-toluene sulphonic acid (165 g) were charged to a heated reactor fitted with a reflux condenser. When the reactor temperature reached 85° C., the intermediate resin (27.5 kg), maintained at about 50° C. to keep the resin mobile, was slowly dripped into the reactor. The resin addition took approximately 1 hour. The temperature of the mixture rose to about 118° C. during the addition. After all the resin had been added, the mixture was heated to about 140° C. and superheated steam at about 150° C. was passed through it to raise the softening point of the phenolated resin. When the softening point of the resin was 105° C. (determined by the Ring and Ball method) the phenolated resin was allowed to cool and was dried. The phenolated resin had the properties given below:
Softening point:105° C.
Free Phenol Content:0.9%
Combined Phenol Content:48%
Oxygen Content:8.3%
Number average molecular weight:1050
The phenolated resin (100 parts) was then dissolved in sufficient IMS to give a 50% solution and hexamine (10 parts) (based on the weight of the phenolated resin) was added thereto. This provided a varnish which was used to make glasscloth laminates.
Five sheets, each 304 mm square were cut from a roll of glasscloth using a sharp knife. Each sheet was placed on a glass plate and about 40 g of varnish poured onto it. A hand roller was drawn across the sheet several times to ensure even impregnation of the fabric and to remove excess varnish.
The impregnated sheets were freely suspended and air dried for about 1 hour after which they were pre-cured for a fixed time in an air circulating oven at 135° C. Each sheet was cut into 4 equal squares and the 20 sheets thus obtained were stacked one of top of each other between plates lined with aluminum foil. The stack of sheets was pressed at 150° C. in a hydraulic press. The initial pressure was 3.4 MN/mm2 which was allowed to fall progressively to 1.13 MN/mm2 over the 1 hour dwell period. At the end of this time the laminate was cooled to room temperature while still under pressure (1.13 MN/mm2) and thereafter removed for post-curing.
Rectangular test pieces 12.5 mm wide and of length approximately 27 times their thickness milled from the cured laminates were supported at one end and freely suspended in an air oven at 175° C. and post-cured as follows.
16 hours at 175° C.
4 hours from 175° C. to 200° C.
21 hours at 200° C.
8 hours from 200° C. to 250° C.
During either the curing or the post-curing of the laminates, blistering and cracking occurred, thereby rendering the artefacts unsuitable for most applications.
Preparation 2--According to the Invention
The method described in Preparation 1 was followed to produce a phenolated toluene formaldehyde (TFP) resin. The TFP resin (100 parts) was then dissolved in butane-2-one (63 parts). Hexamine (10 parts) was dissolved in a minimum amount of water, in this case 14 parts of water, and IMS (23 parts) was added. The hexamine solution was mixed thoroughly to ensure that all the hexamine was dissolved. The TFP resin solution and the hexamine solution were then mixed intimately and filtered through muslin to produce a first varnish according to the invention. The varnish was used to make glass cloth laminates.
Preparation 3--According to the Invention
A similar procedure to that described in the previous paragraph was carried out except that the resin solvent was isopropanol instead of butan-2-one. This produced a second varnish according to the invention.
The method of producing the laminates from the two varnishes according to the invention was the same as that described in Preparation 1, and included the same curing and post-curing schedule. At no time was there any evidence of cracking or blistering whichever varnish according to the invention was used and the laminates maintained their strength throughout the treatment period. Moreover, the cross-breaking strength of the laminates measured at 250° C. was relatively unchanged after ageing for up to 1000 h at 250° C.
The cross breaking strengths of the laminates were measured according to B.S. 2782, Method 304 B, 1970. The result of the measurements are given in the table below, in which comparable results for a laminate made with Xylok-210, a commercially available laminating resin, are also given.
______________________________________                                    
       Cross-breaking Strength (N/mm.sup.2)                               
Resin    After post curing schedule                                       
                          After 1000 h at 250° C.                  
______________________________________                                    
Preparation 2                                                             
         160              220                                             
Preparation 3                                                             
         175              240                                             
Xylok-210                                                                 
         150              260                                             
______________________________________                                    
It can thus be seen that glass cloth laminates made with varnishes according to the invention have equivalent properties to similar laminates made with a commercial resin, such as Xylok-210.

Claims (5)

We claim:
1. A varnish for the preparation of glasscloth laminates, comprising a mixture of:
a solution of 100 parts of a TFP resin having a number average molecular weight of about 1000 and an oxygen content of about 8% dissolved in a solvent selected from the group consisting of C4 to C6 alkanones and C3 or C4 alkanols; and
a solution of from 8 to 12 parts of hexamine dissolved in a minimum amount of a solvent comprising water and a lower alkanol in a ratio of about 3:5.
2. A varnish according to claim 1, wherein the TFP resin contains a small proportion of low molecular weight material.
3. A varnish according to claim 1, wherein the resin solvent is butan-2-one.
4. A varnish according to claim 1, wherein the resin solvent is iso-propanol.
5. A varnish according to claim 1, wherein the lower alkanol in the hexamine solvent is IMS.
US06/311,647 1980-11-07 1981-10-15 Varnishes for glasscloth laminates, methods of their production and laminates made therefrom Expired - Fee Related US4408003A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904516A (en) * 1988-01-12 1990-02-27 Certain Teed Corp Phenol-formaldehyde resin solution containing water soluble alkaline earth metal salt
US5300562A (en) * 1991-05-09 1994-04-05 Certainteed Corporation Process for preparing phenolic binder
US5342430A (en) * 1993-07-28 1994-08-30 Grocela Kathe Teresa A Passivation of methylchlorosilane fines
US6730770B2 (en) 2002-05-31 2004-05-04 Certainteed Corporation Method of preparing a higher solids phenolic resin
US6806343B2 (en) 2002-05-31 2004-10-19 Certainteed Corporation Method of preparing a stable, low pH phenolic resin

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB768699A (en) 1954-05-06 1957-02-20 British Oxygen Co Ltd Improvements in or relating to the production of resin bonded glass-cloth laminates
US3691121A (en) * 1971-03-09 1972-09-12 Monsanto Co Resole varnishes prepared from substituted phenols
DE2519406A1 (en) 1974-05-10 1975-11-20 Coal Industry Patents Ltd PROCESS FOR THE MANUFACTURING OF RESINS OF THE NOVOLAK TYPE, RESINS MANUFACTURED BY THIS PROCESS, VARNISHES CONTAINING THEM, AND ARTICLES IMPREGNATED WITH THE RESINS
EP0017312A1 (en) * 1979-03-02 1980-10-15 Coal Industry (Patents) Limited Method of producing a resin for producing heat stable products, the resin and the products

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2912428A1 (en) * 1979-03-29 1980-10-09 Basf Ag NEW DISPERSION DYES, THEIR PRODUCTION AND USE

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB768699A (en) 1954-05-06 1957-02-20 British Oxygen Co Ltd Improvements in or relating to the production of resin bonded glass-cloth laminates
US3691121A (en) * 1971-03-09 1972-09-12 Monsanto Co Resole varnishes prepared from substituted phenols
DE2519406A1 (en) 1974-05-10 1975-11-20 Coal Industry Patents Ltd PROCESS FOR THE MANUFACTURING OF RESINS OF THE NOVOLAK TYPE, RESINS MANUFACTURED BY THIS PROCESS, VARNISHES CONTAINING THEM, AND ARTICLES IMPREGNATED WITH THE RESINS
EP0017312A1 (en) * 1979-03-02 1980-10-15 Coal Industry (Patents) Limited Method of producing a resin for producing heat stable products, the resin and the products

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904516A (en) * 1988-01-12 1990-02-27 Certain Teed Corp Phenol-formaldehyde resin solution containing water soluble alkaline earth metal salt
US5300562A (en) * 1991-05-09 1994-04-05 Certainteed Corporation Process for preparing phenolic binder
US5342430A (en) * 1993-07-28 1994-08-30 Grocela Kathe Teresa A Passivation of methylchlorosilane fines
US6730770B2 (en) 2002-05-31 2004-05-04 Certainteed Corporation Method of preparing a higher solids phenolic resin
US6806343B2 (en) 2002-05-31 2004-10-19 Certainteed Corporation Method of preparing a stable, low pH phenolic resin

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EP0052420A1 (en) 1982-05-26
GB2087414A (en) 1982-05-26
EP0052420B1 (en) 1986-01-08
GB2087414B (en) 1984-05-10
DE3173463D1 (en) 1986-02-20

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